About The Position

KDC is a network of best-in-class custom formulators and manufacturers of color cosmetics, skincare, haircare, bath & body, fragrance, deodorant, home, health, industrial, and auto care products. KDC delivers high-touch innovation, operational excellence, and speed to market to well-known and emerging beauty, personal, and specialty companies from coast to coast. KDC has its head office in Longueuil, Québec. In addition, KDC has 10 operating facilities located throughout North America. Altogether, the company employs nearly 4,800 talented and dedicated employees in North America. Basic Function: Performs diversified raw material and/or finished product testing according to established procedures and performs development work on new procedures in all areas of the analytical laboratory.

Requirements

  • Two years’ college or equivalent
  • Minimum three years’ industry or related experience in pharmaceutical or medical device.
  • Proven technical skills including experience with laboratory methodologies and equipment.
  • Procedure development and writing skills.
  • Basic Microbiology knowledge.
  • Effective communication skills - internal, contract labs and customer contact
  • Strong computer skills. Ability to work in all Microsoft Office Applications
  • Knowledge of US FDA cGMP, GDP and ISO
  • Ability to multi-task and prioritize with attention to detail.

Responsibilities

  • Conduct OOS lab investigations, CAPA and prepare reports.
  • Write SOPs for the analytical lab.
  • Review Blending batch records and release blends for production.
  • Maintains a working knowledge of raw material control and / orfinished product analysis.
  • May discuss procedural problems with customers and/or interplant personnel.
  • Performs daily raw materialand/or in-process bulk and finished product testing to support production.
  • Operates analytical instrumentation such as IR spectrophotometer,
  • Contributes suggestions for improving laboratory methods and procedures.
  • Performs special project work with minimum supervision.
  • Participates in the analytical in-house education training program.
  • Performs PH, specific gravity and viscosity.
  • Review and verify lab notebooks.
  • Knowledge of USP requirements.
  • Knowledge of wet chemistry and titration
  • Interaction with vendors, particularly securing expiration dates on materials.
  • Maintain calibrations of lab instrumentation.
  • Perform Environmental Testing and initiate OOS investigation.
  • Carry out any additional assignment as directed by the QA manager.
  • of incoming C of A and test procedure
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